Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome

Journal of Clinical Endocrinology and Metabolism

Volumn 85, Issue 2, 2000, Pages 658-665

  Ahmed, S F ^a,b   Cheng, A ^a   Dovey, L ^a   Hawkins, J R ^a   Martin, H ^a   Rowland, J ^a   Shimura, N ^a   Tait, A D ^a   Hughes, I A ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN; ANDROGEN RECEPTOR;

ANDROGEN INSENSITIVITY SYNDROME; ARTICLE; CHILD; DNA SEQUENCE; GENE MUTATION; GENETIC ANALYSIS; GONADECTOMY; HUMAN; MAJOR CLINICAL STUDY; MALE; MASCULINITY; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; RECEPTOR BINDING;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANDROGEN-INSENSITIVITY SYNDROME; BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; GENITALIA, MALE; HUMANS; INFANT; MALE; PHENOTYPE; RECEPTORS, ANDROGEN;

EID: 0034454581     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.85.2.658     Document Type: Article

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